Sandoz México is seeking a Regulatory Affairs professional to support the regulatory submissions and lifecycle management of medicinal products. You will coordinate with COFEPRIS, ensure timelines, and maintain high-quality documentation to support market authorizations.
Idóneo candidates have at least 1 year in Regulatory Affairs, strong attention to detail, and fluency in English to collaborate with global teams across borders.
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📌 Regulatory Affairs Specialist: COFEPRIS Submissions (Ciudad de México)
🏢 Sandoz México
📍 Ciudad de México
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